FDA 510(k)

Vortex5 尖鈎趾修復系統

K 號：K260291 · 2026-03-25

申請人Nvision Biomedical Technologies, Inc.

決定日期2026-03-25

產品代碼HRS

諮詢委員會或

決定相當於

器材摘要

Vortex5 Tailor's Bunion Correction System is the device name listed in this FDA 510(k) record. The listed applicant is Nvision Biomedical Technologies, Inc.. It received FDA 510(k) clearance on 2026-03-25 under 510(k) number K260291. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

常見問題

What is the Vortex5 Tailor's Bunion Correction System?

Vortex5 Tailor's Bunion Correction System is a medical device that received FDA 510(k) clearance on 2026-03-25. The listed applicant is Nvision Biomedical Technologies, Inc.. The 510(k) number is K260291.

When did Vortex5 Tailor's Bunion Correction System receive FDA 510(k) clearance?

Vortex5 Tailor's Bunion Correction System received FDA 510(k) clearance on 2026-03-25, under 510(k) number K260291.

Who is the listed applicant for Vortex5 Tailor's Bunion Correction System?

The FDA 510(k) record lists Nvision Biomedical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Vortex5 Tailor's Bunion Correction System?

The FDA product code for Vortex5 Tailor's Bunion Correction System is HRS.

其他以 Nvision Biomedical Technologies, Inc. 為申請人之記錄

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相關器械（代碼：HRS）

相關紀錄係使用名稱、產品代碼或其他後設資料自動配對。配對結果並不構成已驗證的臨床、科學、企業或監管關係，請查閱連結的官方來源。

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